FDASeptember 15, 2015device

Monaco Radiation Treatment Planning System. Used to make treatment plans for patients with prescriptions for external beam radiation therapy.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Dose and MU are incorrect when CT images are viewed from the head, and, when using multiple prescriptions with forced densities.

What to do

FDA enforcement status: Terminated

Brands named

elekta

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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